Auditing Analytical Laboratories for FDA Compliance 2017

  • 895.00 Dollar US$
  • Published date: September 21, 2017
    • Manila, Philippines, Manila, Philippines, United States


Course "Auditing Analytical Laboratories for FDA Compliance" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted.

Who will benefit:

The following specific types of workers will benefit from this webinar:
• External and Internal Auditors
• Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups
• Supervisors and Analysts in Contract Testing Laboratories
• Personnel Responsible for Selecting Contract Testing Laboratories
• Consultants




Location: Manila, Philippines Date: November 20th & 21st, 2017 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON, Manila, Philippines



Price:

Price: $895.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $2,685.00 $4,475.00 You Save: $1,790.00 (40%)*
Register now and save $200. (Early Bird)
Until October 10, Early Bird Price: $895.00 From October 11 to November 18, Regular Price: $1,095.00
Register for 10 attendees Price: $4,922.00 $8,950.00 You Save: $4,028.00 (45%)*


Contact us today!

NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
support@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com

Registration Link - http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901324SEMINAR?science-marketplace-November-2017-SEO
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